ADDITION REACTIONS OF VINYL PHENYL KETONE. I. PHENYLNITROMETHANE

1929 ◽  
Vol 51 (7) ◽  
pp. 2151-2157 ◽  
Author(s):  
Charles F. H. Allen ◽  
M. Philbrick Bridgess
1934 ◽  
Vol 11 (1) ◽  
pp. 40-46 ◽  
Author(s):  
C. F. H. Allen ◽  
A. C. Bell

Methyl cyanoacctate, cyanoacetamide, and malonitrile readily add to vinyl phenyl ketone to give trimolecular products, while nitromethane gives a substance composed of one molecule of nitro compound and three molecules of unsaturated ketone. The reactions of the delta ketonic nitrile formed from the ester are described in detail; it is transformed into reduced pyridine derivatives, and a secondary open chain nitrile. The latter, in turn, is converted into pyridine and hydropyridine derivatives.


1932 ◽  
Vol 54 (2) ◽  
pp. 736-748 ◽  
Author(s):  
C. F. H. Allen ◽  
W. E. Barker

1940 ◽  
Vol 62 (3) ◽  
pp. 656-664 ◽  
Author(s):  
C. F. H. Allen ◽  
A. C. Bell ◽  
Alan Bell ◽  
James Van Allan

1933 ◽  
Vol 55 (7) ◽  
pp. 2953-2960 ◽  
Author(s):  
C. F. H. Allen ◽  
H. W. J. Cressman

1935 ◽  
Vol 57 (7) ◽  
pp. 1322-1325 ◽  
Author(s):  
C. F. H. Allen ◽  
S. C. Overbaugh

2007 ◽  
Vol 4 (4) ◽  
pp. 281-284 ◽  
Author(s):  
Yanyan Chai ◽  
Dewen Dong ◽  
Yan Ouyang ◽  
Yongjiu Liang ◽  
Yan Wang ◽  
...  

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